Medical Device Process Validation - Statistical Aspects - Webinar By GlobalCompliancePanel 2012
02 May 2012
Webinar
Description
Topics
The Statistical Process Model
QMS Requirements for Process Validation
The Process Input Parameters
The Process Output
Risk Management
Who should Attend
Medical Device professionals including Quality Engineers, Quality Managers, Production Supervisors, Production Managers, Production Engineers, Manufacturing Engineers, Process Owners and Design Engineers.
Past Events
Medical Device Process Validation - Statistical Aspects - Webinar By GlobalCompliancePanel 2012 - 02 May 2012, Webinar (28417)
Important
Please, check "Medical Device Process Validation - Statistical Aspects - Webinar By GlobalCompliancePanel" official website for possible changes, before making any traveling arrangements
Event Categories
Health & Medicine: Healthcare, Medical device, Pharma
